HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → HCID 21081908, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | 1-Benzyl-4,6-dichloro-2-oxo-1,2-dihydroquinoline-3-carbonitrile | HCID 21081904 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21081908 | HCID 21081908 | 98% |
Reaction Steps
A solution of Compound 68 (0.8 g, 2.43 mmol) in dichloromethane was added slowly to a stirred solution of piperazine (628 mg g, 7.29 mmol) in dichloromethane at room temperature. The solution was stirred overnight at room temperature. The solvent was then removed under reduced pressure. The residue was taken in water, sonicated briefly, and filtered. The solids were dissolved in ethyl acetate and washed by water. The organic layer was dried over Na2SO4 and concentrated to yield 0.9 g (98%) of yellow solids. M.P. 156° C. 1H NMR (DMSO-d6): δ 2.94 (m, 4H), 3.55 (m, 4H), 5.47 (s, 2H), 7.19 (m, 2H), 7.24 (m, 1H), 7.31 (m, 2H), 7.39 (d, J=8.9 Hz, 1H), 7.64 (dd, J=2.6, 8.9 Hz, 1H), 7.81 (d, J=2.6 Hz, 1H). EIMS m/z 379 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07173036B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-2c745ac7a1fc4b9abbfb2795045a57ea |
| Source note | uspto-grants-2007_02 |